Driving innovative therapies that transform lives
At Ocupharm, we support the development of new ophthalmology therapies from research to clinical application, ensuring scientific rigor, operational excellence, and a patient-centered approach. Our goal is to transform innovation into solutions that improve people’s vision and quality of life.
Leading clinical trials with precision and confidence.
At Ocupharm, we support the development of innovative ophthalmology therapies that aim to improve patients’ vision and quality of life. We work alongside sponsors, investigators, and clinical sites to ensure that every study is conducted under the highest scientific, ethical, and regulatory standards.
Our expertise in ophthalmic clinical research allows us to offer rigorous and efficient trial management, optimizing processes and ensuring data quality throughout each phase of the study.
- CRO specialized in ophthalmology
- Access to our international network of experienced investigators for high-quality data generation.
- Close collaboration with sponsors across the study lifecycle.
- Patient-centered approach
From the laboratory to the clinical trial
We have over 13 years of experience in ophthalmology studies, providing a solid scientific foundation for the development of new therapies and medical devices.
Our expertise allows us to support the transition of new therapies from experimental evaluation to clinical research in patients, integrating preclinical, methodological, and regulatory knowledge to accelerate the advancement of therapeutic innovation.
- Experience in preclinical and clinical research
- Generation of solid and reproducible scientific evidence
- Development and evaluation of innovative therapies
Clinical expertise in ocular diseases.
We bring together a multidisciplinary team with extensive expertise in the design, coordination, and execution of ophthalmic clinical trials across a range of ocular diseases.
Our in-depth clinical knowledge enables us to tailor each study to the specific requirements of every protocol, optimizing patient recruitment, follow-up, and assessments.
- Comprehensive design and management of ophthalmology studies
- Extensive knowledge of ocular diseases
- Optimization of clinical and operational processes
- Efficient and patient-centered research
Tailored solutions to accelerate your development
Every research project presents unique challenges. At Ocupharm, we develop strategies adapted to the specific needs of each sponsor and project, providing flexible solutions that facilitate the efficient advancement of clinical development in ophthalmology.
We accompany our partners from the early planning phases through execution and regulatory support, providing strategic guidance and specialized expertise in medical devices and ophthalmology therapies.
You can rely on us to provide strategic guidance, optimize study design, and confidently navigate the regulatory landscape.
- We provide advisory support in technical documentation and regulatory strategy.
- We act as a liaison with regulatory authorities, including Notified Bodies.
- We guide you through the CE marking process and regulatory compliance in accordance with Regulations (EU) 2017/745 and (EU) 2017/746.
- We conduct audits and implement quality management systems in compliance with ISO 9001, ISO 13485, and ISO 14155 standards.
Do you have any questions?
Send us your message and we’ll get back to you as soon as possible.